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RECALL RECORD — CLASS IIIRecall closedD-0785-2020/FDA enforcement
Idelle Labs·Cosmetics·Nov 20, 2019

Sure 48hr Confidence Regular Original Solid Anti-perspirant & Deodorant NET WT 2.7 OZ (76g)

What you need to know

Class III

  • What happened

    Labeling Product Contains Undeclared API: Active Ingredient on label is not the active ingredient in the product.

  • Health risk

    The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. An allergen that is present but missing or incorrect on the label can cause a serious reaction in allergic consumers.

  • Action required

    Stop applying or using the product. Check the UPC and lot codes below, then return it to the retailer or contact the manufacturer about a refund or replacement.

Recall closed · classified by the FDANationwide (US)More cosmetics

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Product identification

Source: FDA COSMETICS

Brand nameIdelle Labs
Recalling firmIdelle LabsEl Paso, TX, United States
UPC / barcodes
8 834847 17936 6
Lot / date codes
  • Lots: 19279K1, 19279K2, 19280K1
Distribution area
Nationwide

Nationwide in the USA

United States

Quantity affectedNot provided by the FDA.
Recall initiationFDA report date: January 15, 2020
FDA recall numberD-0785-2020

Beyond the headline

The recall, in context

Idelle Labs initiated this cosmetics recall on November 20, 2019. The FDA enforcement report states: Labeling Product Contains Undeclared API: Active Ingredient on label is not the active ingredient in the product. The FDA report lists distribution as: Nationwide in the USA.

The FDA enforcement report describes the reason as: Labeling Product Contains Undeclared API: Active Ingredient on label is not the active ingredient in the product.

Sure 48hr Confidence Regular Original Solid Anti-perspirant & Deodorant NET WT 2.7 OZ (76g) was made or distributed by Idelle Labs in El Paso, TX, United States. This page reflects FDA report D-0785-2020, dated January 15, 2020.

Why this is a Class III recall

Class III means the product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. In this recall, an allergen that is present but missing or incorrect on the label can cause a serious reaction in allergic consumers.

FDA definition

The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations.

What to do now

  1. 1

    Stop using it

    Set the product aside and do not apply it.

  2. 2

    Check the codes

    Compare the UPC and lot code against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Undeclared allergen

Symptoms to watch for

Hives, swelling, wheezing, coughing, vomiting, abdominal pain or a drop in blood pressure. Anaphylaxis is a medical emergency.

When symptoms may appear

Allergic reactions often begin within minutes to a few hours of eating the allergen.

Higher-risk groups

Anyone with a diagnosed food allergy, especially children, and people with a history of anaphylaxis or asthma.

What to do now

  1. 1Do not eat or serve the affected product if you or anyone in the household has a diagnosed allergy.
  2. 2If symptoms such as swelling, wheezing or breathing difficulty occur, use the person's prescribed emergency plan and call emergency services.
  3. 3Keep the packaging, contact the retailer or manufacturer for a refund, and read the official recall notice for the exact allergen.

For a severe allergic reaction, do not wait for a callback or refund process before seeking emergency care.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Sure 48hr Confidence Regular Original Solid Anti-perspirant & Deodorant NET WT 2.7 OZ (76g) recall?

Idelle Labs recalled Sure 48hr Confidence Regular Original Solid Anti-perspirant & Deodorant NET WT 2.7 OZ (76g) in an FDA Class III enforcement action reported as D-0785-2020. Labeling Product Contains Undeclared API: Active Ingredient on label is not the active ingredient in the product.

What are the symptoms of Undeclared allergen exposure?

Hives, swelling, wheezing, coughing, vomiting, abdominal pain or a drop in blood pressure. Anaphylaxis is a medical emergency.

How quickly can Undeclared allergen symptoms appear?

Allergic reactions often begin within minutes to a few hours of eating the allergen.

Who is most at risk from Undeclared allergen?

Anyone with a diagnosed food allergy, especially children, and people with a history of anaphylaxis or asthma.

What should I do if I bought this product?

Stop applying or using the product. Check the UPC and lot codes below, then return it to the retailer or contact the manufacturer about a refund or replacement. Do not eat or serve the affected product if you or anyone in the household has a diagnosed allergy. If symptoms such as swelling, wheezing or breathing difficulty occur, use the person's prescribed emergency plan and call emergency services. Keep the packaging, contact the retailer or manufacturer for a refund, and read the official recall notice for the exact allergen.

How do I get a refund from Idelle Labs?

Contact the recalling company or the retailer where you purchased the product, quote the FDA recall number and ask about a refund or replacement. Keep the packaging, lot code and proof of purchase where possible. The FDA does not issue consumer refunds. Reference FDA recall D-0785-2020 and keep the packaging, lot code and proof of purchase if you have them.

Is the Idelle Labs recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record D-0785-2020. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Brand history

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.